Hemmerich S, Pecht I
Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
Biochemistry. 1992 May 19;31(19):4580-7. doi: 10.1021/bi00134a007.
Nucleoside diphosphate (NDP) kinases have been found to be involved in a wide range of fundamental biological processes ranging from developmental control to signal transduction and metastasis. We have recently cloned and sequenced a cDNA encoding an NDP-kinase of the rat mucosal mast cell line RBL-2H3 [Hemmerich, S., Yarden, Y., & Pecht, I. (1992) Biochemistry (preceding paper in this issue)]. The enzyme itself has been isolated by means of its affinity to the bischromone cromoglycate. Here we report several of its biochemical characteristics: A structural model for the native protein is proposed in which two disulfide-linked pairs of similar 18-kDa subunits (p18) associate to form a 72-kDa tetramer (p72). This is based on the migration properties of the purified enzyme on gel filtration columns, sodium dodecylsulfate gel electrophoresis, and two-dimensional electrophoresis, together with peptide mapping data. In the absence of NDP, both intact p72 and the dissociated 18-kDa subunits (p18) were shown to undergo Mg(2+)-dependent stoichiometric autophosphorylation utilizing adenosine and guanosine triphosphate or gamma-thiotriphosphate as phosphate donor. This autophosphorylation activity was found to be retained by the 18-kDa subunits even following fractionation by SDS-PAGE and electrophoretic transfer to nitrocellulose. The Michaelis constant of this autophosphorylation reaction with either ATP, ATP gamma S, GTP, or GTP gamma S was determined to be 6.5 +/- 1 microM, and maximally 2 mol of phosphate were found to be incorporated per p72 molecule, thus indicating that phosphorylation occurs at a single site on only two of the four 18-kDa subunits of the holoenzyme.(ABSTRACT TRUNCATED AT 250 WORDS)
核苷二磷酸(NDP)激酶已被发现参与从发育控制到信号转导和转移等广泛的基本生物学过程。我们最近克隆并测序了编码大鼠黏膜肥大细胞系RBL - 2H3的NDP激酶的cDNA[赫默里希,S.,亚登,Y.,&佩希特,I.(1992年)《生物化学》(本期前一篇论文)]。该酶本身已通过其与双色酮色甘酸的亲和力分离出来。在此我们报告其几个生化特性:提出了天然蛋白的结构模型,其中两个由二硫键连接的类似18 kDa亚基(p18)对缔合形成72 kDa四聚体(p72)。这是基于纯化酶在凝胶过滤柱、十二烷基硫酸钠凝胶电泳和二维电泳上的迁移特性,以及肽图谱数据得出的。在没有NDP的情况下,完整的p72和解离的18 kDa亚基(p18)都显示利用腺苷和鸟苷三磷酸或γ-硫代三磷酸作为磷酸供体进行Mg(2 +)依赖性化学计量的自磷酸化。即使经过SDS - PAGE分级分离并电泳转移到硝酸纤维素膜上,18 kDa亚基仍保留这种自磷酸化活性。该自磷酸化反应与ATP、ATPγS、GTP或GTPγS的米氏常数测定为6.5±1μM,并且发现每个p72分子最多掺入2摩尔磷酸盐,因此表明磷酸化仅发生在全酶四个18 kDa亚基中两个亚基的单个位点上。(摘要截短至250字)